5Q9T

PanDDA analysis group deposition -- Crystal Structure of DCLRE1A after initial refinement with no ligand modelled (structure 275)

Experimental procedure

Experimental method	SINGLE WAVELENGTH
Source type	SYNCHROTRON
Source details	DIAMOND BEAMLINE I04-1
Synchrotron site	Diamond
Beamline	I04-1
Detector technology	PIXEL
Collection date	2017-04-12
Detector	DECTRIS PILATUS 6M
Wavelength(s)	0.92
Spacegroup name	P 21 21 21
Unit cell lengths	51.727, 57.130, 114.988
Unit cell angles	90.00, 90.00, 90.00

Refinement procedure

Resolution	51.720 - 1.370
R-factor	0.2057
Rwork	0.204
R-free	0.23420
Structure solution method	FOURIER SYNTHESIS
Starting model (for MR)	5aho
RMSD bond length	0.024
RMSD bond angle	2.103
Data reduction software	XDS
Data scaling software	Aimless (0.5.31)
Phasing software	REFMAC
Refinement software	REFMAC (5.8.0155)

Data quality characteristics

	Overall	Inner shell	Outer shell
Low resolution limit [Å]	51.720	51.720	1.410
High resolution limit [Å]	1.370	6.130	1.370
Rmerge	0.053	0.023	1.377
Rmeas	0.058	0.025	1.543
Rpim	0.023	0.010	0.689
Total number of observations	438423	5625	26096
Number of reflections	72458
<I/σ(I)>	12.6	48.9	1.1
Completeness [%]	100.0	99.9	100
Redundancy	6.1	6	4.9
CC(1/2)	1.000	1.000	0.555

Crystallization Conditions

crystal ID	method	pH	temperature	details
1	VAPOR DIFFUSION, SITTING DROP	6	298	30% PEG 1000, 0.1M MIB buffer